Orthopaedic/craniofacial implantation planning software
United Kingdom·General Medical Device·Peek Health, S.A.·Registered Nov 26, 2024- Device ID
- 183370
- MHRA Reference Number
- 183370
- Date Registered
- Nov 26, 2024
- Last Updated
- Nov 5, 2024
- Device Type
- General Medical Device
- Devices
- Orthopaedic/craniofacial implantation planning software
- Type
- Class IIa
- Address
- Centro de Negócios Ideia Atlântico Rua Padres Carmelitas Braga, Portugal
- Created Date
- Dec 18, 2023
- Name
- CASUS UKRP LTD
- Relationship Type
- UK Responsible Person
- Address
- 107-111 Fleet Street London, England, United KingdomPostcode: EC4A 2AB
Devices with a matching generic name or device type registered with MHRA
Additional devices represented by CASUS UKRP LTD in the UK
Orthopaedic/craniofacial implantation planning software is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 183370. The device is manufactured by Peek Health, S.A. from Portugal, classified as General Medical Device. The authorized representative in the UK is CASUS UKRP LTD.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.